| Symbol |
Name |
|
ACSF3
|
acyl-CoA synthetase family member 3
|
|
ALDH5A1
|
aldehyde dehydrogenase 5 family, member A1
|
|
ALDH6A1
|
aldehyde dehydrogenase 6 family, member A1
|
|
ASL
|
argininosuccinate lyase
|
|
AUH
|
AU RNA binding protein/enoyl-CoA hydratase
|
|
CLPB
|
ClpB homolog, mitochondrial AAA ATPase chaperonin
|
|
D2HGDH
|
D-2-hydroxyglutarate dehydrogenase
|
|
DHTKD1
|
dehydrogenase E1 and transketolase domain containing 1
|
|
ETFDH
|
electron-transferring-flavoprotein dehydrogenase
|
|
ETHE1
|
ethylmalonic encephalopathy 1
|
|
FH
|
fumarate hydratase
|
|
GCDH
|
glutaryl-CoA dehydrogenase
|
|
GLYCTK
|
glycerate kinase
|
|
HMGCL
|
3-hydroxymethyl-3-methylglutaryl-CoA lyase
|
|
IDH2
|
isocitrate dehydrogenase 2 (NADP+), mitochondrial
|
|
L2HGDH
|
L-2-hydroxyglutarate dehydrogenase
|
|
MCEE
|
methylmalonyl CoA epimerase
|
|
MMAA
|
methylmalonic aciduria (cobalamin deficiency) cblA type
|
|
MMAB
|
methylmalonic aciduria (cobalamin deficiency) cblB type
|
|
MMACHC
|
methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria
|
|
MMADHC
|
methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria
|
|
MUT
|
methylmalonyl CoA mutase
|
|
MVK
|
mevalonate kinase
|
|
OPA3
|
optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)
|
|
SERAC1
|
serine active site containing 1
|
|
SLC25A1
|
solute carrier family 25 (mitochondrial carrier; citrate transporter), member 1
|
|
SUCLA2
|
succinate-CoA ligase, ADP-forming, beta subunit
|
|
UMPS
|
uridine monophosphate synthetase
|
